Canonical Allele Identifier: CA645518718

Gene: DSTYK

Linked Data

• ClinVar Variation Id: 2701883
• ClinVar RCV Id: RCV003549911
• COSMIC: COSM2214985 ; COSM2214986

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205160240del , CM000663.2:g.205160240del	GRCh38
NC_000001.10:g.205129368del , CM000663.1:g.205129368del	GRCh37
NC_000001.9:g.203395991del	NCBI36
NG_033904.1:g.56363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367162.8:c.1982del MANE Select	ENSP00000356130.3:p.Gly661AlafsTer?
ENST00000367161.7:c.1982del	ENSP00000356129.3:p.Gly661AlafsTer?
ENST00000367162.7:c.1982del	ENSP00000356130.3:p.Gly661AlafsTer?
ENST00000615388.1:c.365del	ENSP00000478016.1:p.Gly122AlafsTer?
NM_015375.2:c.1982del	NP_056190.1:p.Gly661AlafsTer?
NM_199462.2:c.1982del	NP_955749.1:p.Gly661AlafsTer?
XM_011509392.1:c.1955del	XP_011507694.1:p.Gly652AlafsTer?
XM_011509393.1:c.1397del	XP_011507695.1:p.Gly466AlafsTer?
XM_011509394.1:c.1355del	XP_011507696.1:p.Gly452AlafsTer?
XM_011509392.2:c.1955del	XP_011507694.1:p.Gly652AlafsTer?
XM_011509393.2:c.1397del	XP_011507695.1:p.Gly466AlafsTer?
XM_011509394.2:c.1355del	XP_011507696.1:p.Gly452AlafsTer?
NM_015375.3:c.1982del MANE Select	NP_056190.1:p.Gly661AlafsTer?
NM_199462.3:c.1982del	NP_955749.1:p.Gly661AlafsTer?